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PubPharm (128)
121
Fazio-Londe syndrome in siblings from India with different phenotypes
enthalten in:
Brain & development
| 2018
von
Gowda, V.
|
Udhayabanu, T.
|
Varalakshmi, P.
| +2
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122
Tay-Sachs Disease Presenting as Refractory Epilepsy with Autistic Regression Secondary to a Novel Mutation in HEXA Gene
enthalten in:
Indian journal of pediatrics
| 2018
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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123
A Rare Association of Sturge Weber Syndrome with Neurofibromatosis Type-1
enthalten in:
Indian journal of pediatrics
| 2018
von
Gowda, V.
|
Srinivasan, V.
|
Srinivas, S.
| +1
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124
Biotin Thiamin Responsive Basal Ganglia Disease in Siblings
enthalten in:
Indian journal of pediatrics
| 2018
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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125
Biotin Thiamin Responsive Basal Ganglia Disease in Siblings
enthalten in:
Indian journal of pediatrics
| 2018
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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126
Mucolipidosis Type IV Due to Novel MCOLN1 Mutation
enthalten in:
Indian journal of pediatrics
| 2017
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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127
Biotin Thiamin Responsive Basal Ganglia Disease in Siblings
enthalten in:
Indian journal of pediatrics
| 2017
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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128
Mucolipidosis Type IV Due to Novel MCOLN1 Mutation
enthalten in:
Indian journal of pediatrics
| 2017
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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Indian journal of pediatrics
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Indian pediatrics
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Dystonia
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India
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neurodevelopmental disorders
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Biotin thiamine responsive basal ganglia disease
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570
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Biology
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C19orf12 gene
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Membrane Transport Proteins
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2010-2019
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